Lipogems SPA Aspiration Cannulae — Class II medical device recall Z-0690-2016
Terminated recall by Globalmed Logistix, reported 2016-02-03, distributed in CA, CO, CT, FL, GA, NJ, NY. The cannulae may bend during procedure.
| Recall number | Z-0690-2016 |
|---|---|
| Product type | Medical device |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Globalmed Logistix, Norcross, GA, United States |
| Recall initiated | 2015-12-15 |
| Classified | 2016-01-25 |
| Reported by FDA | 2016-02-03 |
| Terminated | 2016-03-09 |
| Distributed | CA, CO, CT, FL, GA, NJ, NY |
| Quantity | 118 units |
| Lot numbers | 0643, 0732 |
| Model numbers | AR1318 |
| Expiration dates | 2020-04 |
Product
Lipogems SPA Aspiration Cannulae, intended for aspiration of adipose tissue. LGC 13G (13G x 185mm), Sterile.
Reason for recall
The cannulae may bend during procedure.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-0690-2016. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.